Role OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. This role is field-based and requires residing in the same country where the job is located.
What You Will Do
Perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, administer protocol and related study training, evaluate the quality and integrity of study site practices, and manage the progress of assigned studies.
Why It Might Be a Fit
The ideal candidate will have at least 2 years of on-site monitoring experience, good knowledge of clinical research regulatory requirements, and strong therapeutic and protocol knowledge.
Requirements
- Bachelor's Degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
- Good therapeutic and protocol knowledge
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
- Written and verbal communication skills
- Organizational and problem-solving skills
- Effective time and financial management skills
Benefits
- Potential base pay range: $57,500.00 - $226,800.00
- Incentive plans, bonuses, and/or other forms of compensation
- Range of health and welfare and/or other benefits
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